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Formulation optimization of gentamicin loaded Eudragit RS100 microspheres using factorial design study.

机译:使用析因设计研究优化了庆大霉素负载的Eudragit RS100微球的配方优化。

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Gentamicin-Eudragit RS100 microspheres were prepared by modified double emulsion method. A 3(2) full factorial experiment was designed to study the effects of the composition of outer aqueous phase in terms of amount of glycerol (viscosity effect) and sodium chloride (osmotic pressure gradient effect) on the entrapment efficiency and % yield and microsphere size. The results of analysis of variance test for responses measured indicated that the test is significant (p>0.05). The contribution of sodium chloride concentration was found to be higher on entrapment efficiency and % yield, whereas glycerol produced significant effect on the mean diameter of microspheres. Microspheres demonstrated spherical particles in the size range of 33.24-60.43 microm. In vitro release profile of optimized formulation demonstrated sustained release for 24 h following Higuchi kinetics. Finally, drug bioactivity was found to remain intact after microencapsulation. Response surface graphs are presented to examine the effectsof independent variables on the responses studied. Thus, by formulation design important parameters affecting formulation characteristics of gentamicin loaded Eudragit RS100 microspheres can be identified for controlled delivery with desirable characters in terms of maximum entrapment and yield.
机译:庆大霉素-Eudragit RS100微球采用改进的双乳化法制备。设计了一个3(2)全因子实验,以研究甘油含量(粘度效应)和氯化钠(渗透压梯度效应)对包封效率,产率%和微球尺寸的影响,研究外部水相的组成。方差检验对所测响应的分析结果表明,检验显着(p> 0.05)。发现氯化钠浓度对包封效率和产率%的贡献更高,而甘油对微球的平均直径产生显着影响。微球显示出球形颗粒,尺寸范围为33.24-60.43微米。优化配方的体外释放曲线表明,Higuchi动力学后可持续释放24小时。最后,发现微囊化后药物生物活性保持完整。给出了响应面图以检查独立变量对所研究响应的影响。因此,通过制剂设计,可以确定影响庆大霉素负载的Eudragit RS100微球制剂特性的重要参数,以便在最大截留量和产率方面具有理想特性的受控递送。

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